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FDA 510(k)

OHIO 7000 ELECTRONIC ANESTHESIA VENTIL.

K-Number: K821376 · 1982-06-29

Decision Date1982-06-29
Product CodeCBK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

OHIO 7000 ELECTRONIC ANESTHESIA VENTIL. is the device name listed in this FDA 510(k) record. The listed applicant is Ohio Medical Products. It received FDA 510(k) clearance on 1982-06-29 under 510(k) number K821376. The device is classified under product code CBK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OHIO 7000 ELECTRONIC ANESTHESIA VENTIL.?

OHIO 7000 ELECTRONIC ANESTHESIA VENTIL. is a medical device that received FDA 510(k) clearance on 1982-06-29. The listed applicant is Ohio Medical Products. The 510(k) number is K821376.

When did OHIO 7000 ELECTRONIC ANESTHESIA VENTIL. receive FDA 510(k) clearance?

OHIO 7000 ELECTRONIC ANESTHESIA VENTIL. received FDA 510(k) clearance on 1982-06-29, under 510(k) number K821376.

Who is the listed applicant for OHIO 7000 ELECTRONIC ANESTHESIA VENTIL.?

The FDA 510(k) record lists Ohio Medical Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OHIO 7000 ELECTRONIC ANESTHESIA VENTIL.?

The FDA product code for OHIO 7000 ELECTRONIC ANESTHESIA VENTIL. is CBK.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Ohio Medical Products as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 47 devices →

Related Devices (Code: CBK)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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